115905-43-6 Usage
General Description
2-BROMO-1-METHYL-1H-IMIDAZOLE-4,5-DICARBONITRILE is a chemical compound that belongs to the class of imidazole derivatives. It is a white to pale yellow crystalline substance with the molecular formula C5H3BrN4. 2-BROMO-1-METHYL-1H-IMIDAZOLE-4,5-DICARBONITRILE is primarily used as an intermediate in organic synthesis, particularly in the manufacture of pharmaceuticals and agrochemicals. It possesses both bromo and cyano functional groups, making it useful in various chemical reactions and as building blocks for more complex compounds. Additionally, it has potential applications in the field of materials science and research. Overall, 2-BROMO-1-METHYL-1H-IMIDAZOLE-4,5-DICARBONITRILE has versatile and valuable properties that make it a significant compound in the chemical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 115905-43-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,9,0 and 5 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 115905-43:
(8*1)+(7*1)+(6*5)+(5*9)+(4*0)+(3*5)+(2*4)+(1*3)=116
116 % 10 = 6
So 115905-43-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H3BrN4/c1-11-5(3-9)4(2-8)10-6(11)7/h1H3
115905-43-6Relevant articles and documents
Synthesis and properties of push-pull imidazole derivatives with application as photoredox catalysts
Hlouková, Zuzana,Bure, Filip
, p. 330 - 342 (2017/06/19)
Two new push-pull molecules with imidazole-4,5-dicarbonitrile acceptor, thiophene and 2-methoxythiophene donors with potential use in photoredox catalysis were designed and prepared. The synthesis started from commercially available imidazole-4,5-dicarbon
New acetylenic monomers and polymers from 4,5-dicyanoimidazole
Densmore, Crystal G.,Rasmussen, Paul G.
, p. 5900 - 5910 (2007/10/03)
An efficient synthesis of 1-methyl-2-ethynyl-4,5-dicyanoimidazole via Sonogashira coupling is described. Our optimized method generates 1-methyl-2-ethynyl-4,5-dicyanoimidazole in almost 80% yield from 1-methyl-2-bromo-4,5-dicyanoimidazole. Syntheses of th
